Development of an immunochromatographic test with anti-LipL32-coupled gold nanoparticles for Leptospira detection

被引:0
作者
Chirathaworn, Chintana [1 ]
Janwitthayanan, Weena [2 ]
Sereemaspun, Amornpun [3 ]
Lertpocasombat, Kanchake [1 ]
Rungpanich, Utane [4 ]
Ekpo, Pattama [4 ]
Suwancharoen, Duangjai [5 ]
机构
[1] Chulalongkorn Univ, Fac Med, Dept Microbiol, Bangkok 10300, Thailand
[2] Chulalongkorn Univ, Fac Med, Master Sci Program Med Sci, Bangkok 10300, Thailand
[3] Chulalongkorn Univ, Fac Med, Dept Anat, Bangkok 10300, Thailand
[4] Chulalongkorn Univ, Fac Med, Dept Immunol, Bangkok 10300, Thailand
[5] Natl Inst Anim Hlth, Dept Livestock Dev, Bangkok, Thailand
关键词
Leptospirosis; LipL32; Diagnosis; Immunochromatography; OUTER-MEMBRANE PROTEIN; IGM-ELISA; PATHOGENIC LEPTOSPIRES; AGGLUTINATION-TEST; DRI-DOT; DIAGNOSIS; PCR; ANTIGEN; LIPL32; SERODIAGNOSIS;
D O I
暂无
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Detection of antibody specific to Leptospira by various immunological techniques has been used for leptospirosis diagnosis. However, the sensitivity of antibody detection during the first few days after infection is low. Molecular techniques are suggested to provide earlier diagnosis than antibody detection, but a rapid and easy to perform assay for Leptospira antigen detection would provide an additional useful tool for disease diagnosis. In this study, we coupled gold nanoparticles with antibody to LipL32, a protein commonly found in pathogenic Leptospira. This coupled gold reagent was used in the immunochromatographic strip for Leptospira detection. We demonstrated that the sensitivity of Leptospira detection by this strip was 10(3) ml(-1). There was no positive result detected when strips were tested with non-pathogenic Leptospira, Staphylococcus aureus, Streptococcus group B, Acinetobacter baumannii, Escherichia coli, Salmonella typhi, Klebsiella pneumoniae, Enterococcus faecalis or Enterococcus faecium. These data suggest that gold nanoparticles coupled with antibody to LipL32 could be used for Leptospira detection by a rapid test based on an immunochromatographic technique.
引用
收藏
页码:201 / 207
页数:7
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